Supramolecular chemistry has garnered important interest in recent years toward improving therapeutic efficacy via drug delivery approaches. Although self-assemblies have been deeply investigated, the design of novel drugs leveraging supramolecular chemistry is less known. In this contribution, we show that a Low Molecular Weight Gel (LMWG) can elicit cancer cell apoptosis. This biological effect results from the unique supramolecular properties of a bolaamphiphile-based gelator, which allow for strong interaction with the lipid membrane. This novel supramolecular-drug paradigm opens up new possibilities for therapeutic applications targeting membrane lipids.Si-doped graphene nanosheets (SiGNS) have been successfully constructed via high temperature annealing of graphene oxide and tetraethoxysilane mixture in a sealed glass ampoule. https://www.selleckchem.com/products/indy.html The Si atoms doped into graphene's carbon network mainly existed as C3-Si-O and C2-Si-O2 configurations. The as-prepared SiGNS exhibited excellent electrochemical detection ability to nitroaromatic compounds in 0.1 M phosphoric acid buffer solution (PBS, pH = 8.0) via an electrochemical catalytic process. Five nitroaromatic compounds, including nitrobenzene, 2-nitrotoluene, 4-nitrotoluene, 2, 4-dinitrotoluene and 2, 4, 6-trinitrotoluene, were taken as the analyte to demonstrate the electrochemical catalytic ability of SiGNS. Density functional theory (DFT) calculation was carried out to explore the electrochemical catalytic mechanism of SiGNS. A hydrogen bond mediated electrochemical catalytic mechanism was proposed. Both the excellent electrical conductivity and the rich surface hydroxyl groups enhanced the electrochemical detection ability of SiGNS to nitroaromatic compounds. Si atoms in SiGNS played a key role for the excellent electrochemical detection ability of SiGNS due to most of the surface hydroxyl groups anchored on the Si atoms.Magnesium (Mg) alloy has wide potential applications due to its unique properties, but is apt to corrosion. Recently, superhydrophobic coatings are receiving great interest for corrosion protection of metals but suffer from short lifespan. Here, we report a strategy for long-term corrosion protection of Mg alloy by designing two-layer self-healing superamphiphobic coatings based on shape memory polymers (SMP) and attapulgite. The superamphiphobic coatings are composed of a bottom SMP coating containing a corrosion inhibitor (1, 2, 3-benzotriazole, BTA) and ceresine wax microparticles and a top superamphiphobic attapulgite coating. The two-layer self-healing coatings have excellent superamphiphobicity and initial anti-corrosion performance. The Mg alloy with the coatings can withstand immersion in 3.5 wt% NaCl solution for 80 days and neutral salt spray with 5 wt% NaCl for 54 days. Furthermore, the coatings show excellent self-healing capability towards various physical damages, such as 10 scratching/self-healing cycles at the same position, hexagonal star scratching and grid scratching. Moreover, the physically damaged coatings exhibit self-healing behavior of the microstructure and superhydrophobicity, driven by the shape memory effect of the bottom SMP layer. Thus, the self-healed coatings can still withstand 60 days of 3.5 wt% NaCl solution immersion and 30 days of 5 wt% NaCl salt spray. This study paves the way for applying super anti-wetting coatings for long-term corrosion protection of metals.The achievement of superlow friction is vital for the engineering application of hydrogenated diamond-like carbon (H-DLC), but it always fails in an oxygen atmosphere. In this paper, robust superlow friction was achieved by MoS2 flakes and H-DLC composite films in a large range of atmospheres, especially in oxygen. The results showed that the composite structure could only retain the superlow friction for an short time in pure argon, nitrogen and carbon dioxide; surprisingly, oxygen was capable of remaining in the near frictionless state with a friction coefficient as low as 0.002, and the duration was prolonged significantly by the introduction of oxygen in those other gases. The stability of the transfer film that induced the near frictionless state was also studied comprehensively. The experimental results and first-principle calculations demonstrated that oxygen could bond with the molybdenum, sulfur and aluminum atoms to form bridge bonds that fixed the MoS2 transfer film on the counterface; this led to the formation of incommensurate contact between the MoS2 tribo-layer and H-DLC film, which enabled robust superlow friction. This finding supports a simple strategy to resolve the challenge of superlubric failure and opens a path for the actual application of H-DLC in oxygen-rich environments.A novel and facile strategy is developed to tune parallel manganese dioxide (MnO2) to hollow parallel hydroxyl oxidize iron (FeOOH) replicas, which can exactly keep its original morphology. The key factors leading to the morphology-preserved transformation are the low-temperature and dropwise strategy via a serial of controlled experiments. Benefiting from the characteristics of parallel and hollow structures, the FeOOH replica delivers remarkable specific capacitance of 186.8F g-1 at 0.5 A g-1. The electrochemical performances delivered by the asymmetric supercapacitor (parallel MnO2//hollow parallel FeOOH) are much superior to those where conventional activated graphene or FeOOH nanoneedles are used as negative electrode materials. This can be attributed to the advantages of parallel nanostructure and high electrochemical matching effect of positive and negative electrode materials. The energy density is recorded up to 46.8 Wh kg-1 at the power density of 0.5 kW kg-1, while it still remains 20.7 Wh kg-1 with the maximum power density of 10 kW kg-1. Furthermore, this strategy shows great universality and can be broadened to almost all MnO2 related researches to synthesize ideal negative electrode materials with high structural and electrochemical matching effect, thus further enhances the electrochemical performances of as-prepared asymmetric supercapacitor devices.It has been recently shown that, in our organism, the secretions of Ca, Mgand phosphate ions lead to the precipitation of amorphous magnesium-calcium phosphate nanoparticles (AMCPs) in the small intestine, where the glycoprotein mucin is one of the most abundant proteins, being the main component of the mucus hydrogel layer covering gut epithelium. Since AMCPs precipitate in vivo in a mucin-rich environment, we aim at studying the effect of this glycoprotein on the formation and features of endogenous-like AMCPs.
AMCPs were synthesized from aqueous solution in the presence of different concentrations of mucin, and the obtained particles were characterised in terms of crystallinity, composition and morphology. Solid State NMR investigation was also performed in order to assess the interplay between mucin and AMCPs at a sub-nanometric level.
Results show that AMCPs form in the presence of mucin and the glycoprotein is efficiently incorporated in the amorphous particles. NMR indicates the existence of interactions between AMCPs and mucin, revealing how AMCPs in mucin-hybrid nanoparticles affect the features of both proteic and oligosaccharidic portions of the glycoprotein.